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Items: 1 to 20 of 188

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3807172copy number variation1estd192human GRCh37 chr9: 35,905,719-35,905,829 , GRCh38.p12 chr9: 35,905,722-35,905,832 HRCT1
    nsv4178998copy number variation1nstd166human GRCh37.p13 chr9: 35,906,547-35,906,634 , GRCh38.p12 chr9: 35,906,550-35,906,637 HRCT1
    nsv7138681insertion1nstd232human GRCh37.p13 chr9: 35,906,601-35,906,601 , GRCh38.p12 chr9: 35,906,604-35,906,604 HRCT1
    nsv6282957insertion1nstd214human GRCh38 chr9: 35,906,563-35,906,563 , GRCh37.p13 chr9: 35,906,560-35,906,560 HRCT1
    nsv6275907insertion2nstd214human GRCh38 chr9: 35,906,568-35,906,568 , GRCh37.p13 chr9: 35,906,565-35,906,565 HRCT1
    nsv6225647insertion2nstd214human GRCh38 chr9: 35,906,604-35,906,604 , GRCh37.p13 chr9: 35,906,601-35,906,601 HRCT1
    nsv6081616insertion1nstd212human GRCh38 chr9: 35,906,589-35,906,589 , GRCh37.p13 chr9: 35,906,586-35,906,586 HRCT1
    nsv4768268insertion1nstd199human GRCh37 chr9: 35,906,607-35,906,607 , GRCh38.p12 chr9: 35,906,610-35,906,610 HRCT1
    nsv5639691insertion1nstd207human GRCh38 chr9: 35,906,592-35,906,592 , GRCh37.p13 chr9: 35,906,589-35,906,589 HRCT1
    nsv5625949insertion1nstd207human GRCh38 chr9: 35,906,568-35,906,568 , GRCh37.p13 chr9: 35,906,565-35,906,565 HRCT1
    nsv3931136insertion1nstd167human GRCh37 chr9: 35,906,601-35,906,601 , GRCh38.p12 chr9: 35,906,604-35,906,604 HRCT1
    nsv3548860insertion1nstd152human GRCh38 chr9: 35,906,581-35,906,581 , GRCh37.p13 chr9: 35,906,578-35,906,578 HRCT1
    nsv3548117insertion1nstd152human GRCh38 chr9: 35,906,589-35,906,589 , GRCh37.p13 chr9: 35,906,586-35,906,586 HRCT1
    nsv3411460insertion1nstd162human GRCh38 chr9: 35,906,576-35,906,576 , GRCh37.p13 chr9: 35,906,573-35,906,573 HRCT1
    nsv2819670insertion1nstd137human GRCh38 chr9: 35,906,576-35,906,576 , GRCh37.p13 chr9: 35,906,573-35,906,573 HRCT1
    nsv2617871short tandem repeat2nstd128human GRCh37 chr9: 35,906,348-35,906,368 , GRCh38.p12 chr9: 35,906,351-35,906,371 HRCT1
    nsv2617870short tandem repeat1nstd128human GRCh37 chr9: 35,904,600-35,904,616 , GRCh38.p12 chr9: 35,904,603-35,904,619 HRCT1
    nsv3965190insertion1nstd168human GRCh38 chr9: 35,895,775-35,929,441 , GRCh37.p13 chr9: 35,895,772-35,929,438 HRCT1, SPAAR
    nsv6448354copy number variation1nstd223human GRCh38 chr9: 35,899,101-35,963,900 , GRCh37.p13 chr9: 35,899,098-35,963,897 HRCT1, SPAAR, 2 more genes
    nsv4604795copy number variation1nstd183human GRCh37 chr9: 35,905,326-35,964,362 , GRCh38.p12 chr9: 35,905,329-35,964,365 HRCT1, SPAAR, 2 more genes
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